Beyond the amyloid hypothesis: how current research implicates autoimmunity in Alzheimer's disease pathogenesis.

IF 6.6 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Miyo K Chatanaka, Dorsa Sohaei, Eleftherios P Diamandis, Ioannis Prassas
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引用次数: 3

Abstract

The amyloid hypothesis has so far been at the forefront of explaining the pathogenesis of Alzheimer's Disease (AD), a progressive neurodegenerative disorder that leads to cognitive decline and eventual death. Recent evidence, however, points to additional factors that contribute to the pathogenesis of this disease. These include the neurovascular hypothesis, the mitochondrial cascade hypothesis, the inflammatory hypothesis, the prion hypothesis, the mutational accumulation hypothesis, and the autoimmunity hypothesis. The purpose of this review was to briefly discuss the factors that are associated with autoimmunity in humans, including sex, the gut and lung microbiomes, age, genetics, and environmental factors. Subsequently, it was to examine the rise of autoimmune phenomena in AD, which can be instigated by a blood-brain barrier breakdown, pathogen infections, and dysfunction of the glymphatic system. Lastly, it was to discuss the various ways by which immune system dysregulation leads to AD, immunomodulating therapies, and future directions in the field of autoimmunity and neurodegeneration. A comprehensive account of the recent research done in the field was extracted from PubMed on 31 January 2022, with the keywords "Alzheimer's disease" and "autoantibodies" for the first search input, and "Alzheimer's disease" with "IgG" for the second. From the first search, 19 papers were selected, because they contained recent research on the autoantibodies found in the biofluids of patients with AD. From the second search, four papers were selected. The analysis of the literature has led to support the autoimmune hypothesis in AD. Autoantibodies were found in biofluids (serum/plasma, cerebrospinal fluid) of patients with AD with multiple methods, including ELISA, Mass Spectrometry, and microarray analysis. Through continuous research, the understanding of the synergistic effects of the various components that lead to AD will pave the way for better therapeutic methods and a deeper understanding of the disease.

超越淀粉样蛋白假说:当前研究如何暗示阿尔茨海默病发病机制中的自身免疫。
淀粉样蛋白假说到目前为止一直是解释阿尔茨海默病发病机制的前沿,阿尔茨海默病是一种进行性神经退行性疾病,会导致认知能力下降和最终死亡。然而,最近的证据指出了导致这种疾病发病的其他因素。这些假说包括神经血管假说、线粒体级联假说、炎症假说、朊病毒假说、突变积累假说和自身免疫假说。本综述的目的是简要讨论与人类自身免疫相关的因素,包括性别、肠道和肺部微生物组、年龄、遗传和环境因素。随后,研究人员研究了AD中自身免疫现象的增加,这可能是由血脑屏障破坏、病原体感染和淋巴系统功能障碍引起的。最后,讨论了免疫系统失调导致AD的各种途径,免疫调节疗法,以及自身免疫和神经退行性变领域的未来方向。2022年1月31日,从PubMed中提取了该领域近期研究的综合说明,第一个搜索输入的关键词是“阿尔茨海默病”和“自身抗体”,第二个搜索输入的关键词是“阿尔茨海默病”和“IgG”。从第一次搜索中,19篇论文被选中,因为它们包含了对阿尔茨海默病患者体液中发现的自身抗体的最新研究。从第二次检索中,选择了四篇论文。对文献的分析支持AD的自身免疫假说。采用ELISA、质谱分析、微阵列分析等多种方法在AD患者的生物体液(血清/血浆、脑脊液)中发现自身抗体。通过不断的研究,了解导致AD的各种成分的协同作用将为更好的治疗方法和对疾病的更深入了解铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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